warnings
Other Ingredients Maize starch, Microcrystalline Cellulose, Magnesium Stearate.
JBA Joint Revive
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- JBA Joint Revive
- Generic name
- GLUCOSAMINE SULFATE POTASSIUM CHLORIDE,WHITE WILLOW BARK EXTRACT,EGGSHELL MEMBRANE COLLAGEN,CHONDROITIN SULFATE,TURMERIC ROOT EXTRACT,BROMELAIN,SOY LECITHIN
- Manufacturer
- Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 27f5acf3-04f6-49d7-bbf5-f1c3ad6200cc
- SPL ID
- 31a5f8ac-00b3-b780-e063-6294a90ac75e
- Version
- 2
- Effective date
- 2025-03-31
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:26:31
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | JBA Joint Revive | openfda.brand_name | |
| generic name | GLUCOSAMINE SULFATE POTASSIUM CHLORIDE,WHITE WILLOW BARK EXTRACT,EGGSHELL MEMBRANE COLLAGEN,CHONDROITIN SULFATE,TURMERIC ROOT EXTRACT,BROMELAIN,SOY LECITHIN | openfda.generic_name | |
| manufacturer name | Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals | openfda.manufacturer_name | |
| ndc | package | 13411-856-15 | openfda.package_ndc |
| ndc | package | 13411-856-30 | openfda.package_ndc |
| ndc | package | 13411-856-60 | openfda.package_ndc |
| ndc | product | 13411-856 | openfda.product_ndc |
| ndc11 | package | 13411085660 | derived:openfda.package_ndc |
| ndc11 | package | 13411085615 | derived:openfda.package_ndc |
| ndc11 | package | 13411085630 | derived:openfda.package_ndc |
| spl id | 31a5f8ac-00b3-b780-e063-6294a90ac75e | id | |
| spl set id | 27f5acf3-04f6-49d7-bbf5-f1c3ad6200cc | set_id | |
| unii | 6IC1M3OG5Z | openfda.unii | |
| unii | N7QBR4212V | openfda.unii | |
| unii | 856YO1Z64F | openfda.unii | |
| unii | ZLM4P8929R | openfda.unii | |
| unii | 205MXS71H7 | openfda.unii | |
| unii | 1DI56QDM62 | openfda.unii | |
| unii | 15VQ11I66N | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.